292 research outputs found
Large eddy simulation of a turbulent flow in a 5 x 5 rod bundle with a mixing vane spacer grid
In fuel assemblies of pressurized water reactors (PWRs), mixing-vane spacer grids are extensively employed to array fuel rods and enhance inter- and intra-subchannel mixing. The turbulent flow downstream of spacer grids is essential knowledge to support the design of spacer grids and mixing vanes. As a high-fidelity approach for turbulence simulation, large eddy simulation (LES) results are assessed with the high-resolution flow field measured with particle image velocimetry (PIV). The LES results reveal a mixing vane effect on vortex structures and Reynolds stresses. The mechanism of vortex generation at the mixing vanes and the development downstream of the spacer grid are visualized by the Q-criterion. The distributions of the root mean square fluctuating velocity and Reynolds stresses decay rapidly downstream of the spacer grid. The secondary flow intensity downstream of the spacer grid predicted by LES is evaluated and follows an exponentially decaying law with distance from the spacer grid
A meta-analysis of genome-wide association studies of multiple myeloma among men and women of African ancestry
Adversarial Attacks and Defenses for Semantic Communication in Vehicular Metaverses
For vehicular metaverses, one of the ultimate user-centric goals is to
optimize the immersive experience and Quality of Service (QoS) for users on
board. Semantic Communication (SemCom) has been introduced as a revolutionary
paradigm that significantly eases communication resource pressure for vehicular
metaverse applications to achieve this goal. SemCom enables high-quality and
ultra-efficient vehicular communication, even with explosively increasing data
traffic among vehicles. In this article, we propose a hierarchical
SemCom-enabled vehicular metaverses framework consisting of the global
metaverse, local metaverses, SemCom module, and resource pool. The global and
local metaverses are brand-new concepts from the metaverse's distribution
standpoint. Considering the QoS of users, this article explores the potential
security vulnerabilities of the proposed framework. To that purpose, this study
highlights a specific security risk to the framework's SemCom module and offers
a viable defense solution, so encouraging community researchers to focus more
on vehicular metaverse security. Finally, we provide an overview of the open
issues of secure SemCom in the vehicular metaverses, notably pointing out
potential future research directions
GDNF secreted from adipose-derived stem cells stimulates VEGF-independent angiogenesis
Adipose tissue stroma contains a population of mesenchymal stem cells (MSC) promote new blood vessel formation and stabilization. These adipose-derived stem cells (ASC) promote de novo formation of vascular structures in vitro. We investigated the angiogenic factors secreted by ASC and discovered that glial-derived neurotrophic factor (GDNF) is a key mediator for endothelial cell network formation. It was found that both GDNF alone or present in ASC-conditioned medium (ASC-CM) stimulated capillary network formation by using human umbilical vein endothelial cells (HUVECs) and such an effect was totally independent of vascular endothelial growth factor (VEGF) activity. Additionally, we showed stimulation of capillary network formation by GDNF, but not VEGF, could be blocked by the Ret (rearranged during transfection) receptor antagonist RPI-1, a GDNF signaling inhibitor. Furthermore, GDNF were found to be overexpressed in cancer cells that were resistant to the anti-angiogenic treatment using the VEGF antibody. Cancer cells in the liver hepatocellular carcinoma (HCC), a non-nervous related cancer, highly overexpressed GDNF as compared to normal liver cells. Our data strongly suggest that, in addition to VEGF, GDNF secreted by ASC and HCC cells, may be another important factor promoting pathological neovascularization. Thus, GDNF may be a potential therapeutic target for HCC and obesity treatments
Magnetic Domain Structure in Ferromagnetic Kagome Metal DyMn6Sn6
Two types of magnetic domains, that is, type-I domain belt domain and type-II new stripe domain, are observed in a kagome metal DyMn6Sn6 by microscopic magneto-optic Kerr imaging technique. From 255 to 235 K, the spin reorientation is observed directly in DyMn6Sn6. We analyze the structure of two types of domains through brightness distribution of the images. The type-II domain exists from 235 to 160 K by zero-field cooling (ZFC). At the same time, type-I domain and type-II domain coexist and transform into each other with variation of temperature. Type-II domains can easily transform into type-I domains when the temperature and magnetic field changes, and this process is irreversible. These results demonstrate that the type-I domain is more stable than the type-II domain. The phase diagram of magnetic domains in DyMn6Sn6 is obtained
Particle triggered reactions as an important mechanism of alkalinity and inorganic carbon removal in river plumes
Author Posting. © American Geophysical Union, 2021. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 48(11), (2021): e2021GL093178, https://doi.org/10.1029/2021GL093178.The effects of heterogeneous reactions between river-borne particles and the carbonate system were studied in the plumes of the Mississippi and Brazos rivers. Measurements within these plumes revealed significant removal of dissolved inorganic carbon (DIC) and total alkalinity (TA). After accounting for all known DIC and TA sinks and sources, heterogeneous reactions (i.e., heterogeneous CaCO3 precipitation and cation exchange between adsorbed and dissolved ions) were found to be responsible for a significant fraction of DIC and TA removal, exceeding 10% and 90%, respectively, in the Mississippi and Brazos plume waters. This finding was corroborated by laboratory experiments, in which the seeding of seawater with the riverine particles induced the removal of the DIC and TA. The combined results demonstrate that heterogeneous reactions may represent an important controlling mechanism of the seawater carbonate system in particle-rich coastal areas and may significantly impact the coastal carbon cycle.This research was funded by the National Science Foundation (NSF) and the Bi-National Science Foundation U.S-Israel award number OCE-BSF 1635388.2021-11-2
Abnormal expression of an ADAR2 alternative splicing variant in gliomas downregulates adenosine-to-inosine RNA editing
BACKGROUND: RNA editing is catalyzed by adenosine deaminases acting on RNA (ADARs). ADAR2 is the main enzyme responsible for recoding editing in humans. Adenosine-to-inosine (A-to-I) editing at the Q/R site is reported to be decreased in gliomas; however, the expression of ADAR2 mRNA was not greatly affected. METHODS: We determined ADAR2 mRNA expression in human glioblastoma cell lines and in normal human glial cells by real-time RT-PCR. We also determined ADAR2 mRNA expression in 44 glioma tissues and normal white matter. After identifying an alternative splicing variant (ASV) of ADAR2 in gliomas, we performed sequencing. We then classified glioblastomas based on the presence (+) or absence (–) of the ASV to determine the correlations between ASV + and malignant features of glioblastomas, such as invasion, peritumoral brain edema, and survival time. RESULTS: There were no significant differences in ADAR2 mRNA expression among human glioblastoma cell lines or in gliomas compared with normal white matter (all p > 0.05). The ASV, which contained a 47-nucleotide insertion in the ADAR2 mRNA transcript, was detected in the U251 and BT325 cell lines, and in some glioma tissues. The expression rate of ASV differed among gliomas of different grades. ASV + glioblastomas were more malignant than ASV – glioblastomas. CONCLUSIONS: ADAR2 is a family of enzymes in which ASVs result in differences in enzymatic activity. The ADAR2 ASV may be correlated with the invasiveness of gliomas. Identification of the mechanistic characterization of ADAR2 ASV may have future potential for individualized molecular targeted-therapy for glioma
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